meddevicedb.com FDA Device Reference

PRESSURE MANOMETER

K841071 Class II Traditional
Decision Date
1984-04-17
Sponsor / Applicant
Interventional Medical, Inc.

Technical Specification

510(k) Submission ID K841071
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1984-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRESSURE MANOMETER received FDA 510(k) clearance under submission number K841071, sponsored by Interventional Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.